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510(k) K872388

NAIL SET by Med-Tool, Inc. — Product Code LRY

K872388 is an FDA 510(k) premarket notification submitted by Med-Tool, Inc. for the device "NAIL SET". The FDA issued a decision of Substantially Equivalent on July 23, 1987. The device falls under product code LRY (Punch, Surgical), a Class I device regulated under 21 CFR 878.4800. Med-Tool, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 23, 1987
Date Received
June 19, 1987
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Punch, Surgical
Device Class
Class I
Regulation Number
878.4800
Review Panel
SU
Submission Type

Other clearances by Med-Tool, Inc.

  • K874357 — TAPERED PUNCH (November 23, 1987)
  • K874356 — PIN PUNCH (November 23, 1987)
  • K874359 — ADJUSTABLE WRENCHES (November 23, 1987)
  • K874358 — COMBINATION WRENCHES (November 23, 1987)
  • K872387 — STANDARD SCREW DRIVER (July 16, 1987)
  • K872385 — VICE OR BENCH VICE (July 16, 1987)
  • K872389 — PRECISION SCREW DRIVER SET (July 15, 1987)
  • K872384 — SIDE CUTTING PARALLEL ACTION PLIERS (July 2, 1987)
  • K872386 — C CLAMP (July 2, 1987)
  • K864019 — NEEDLE NOSE PLIERS (October 30, 1986)

Other clearances for product code LRY

  • K933516 — ACU-E PUNCH (March 24, 1994)
  • K904869 — ELLIPSE PUNCH (March 6, 1991)
  • K902636 — LIPOGEN RHEUMELISA DSDNA ASSAY (June 28, 1990)
  • K896303 — BIOPSY PUNCH (February 13, 1990)
  • K874356 — PIN PUNCH (November 23, 1987)
  • K874357 — TAPERED PUNCH (November 23, 1987)

FDA data resources